MOTOBAND Instruments

FDA UDI

Class I (US FDA UDI)

by Crossroads Extremity Systems Llc

Identity

Trade Name: MOTOBAND Instruments FDA UDI
Generic Name: Surgical implant template, reusable FDA UDI
Device Name: MTP TEMPLATE - STANDARD 5 FDA UDI
Model / Reference: MTP TEMPLATE - STANDARD 5 FDA UDI
Description: MTP TEMPLATE - STANDARD 5 FDA UDI

Identifiers

Catalog Number: TEM261222PKG FDA UDI
Primary DI / UDI-DI: 00810112598704 FDA UDI
FDA Product Code: HWT FDA UDI
GMDN Term: Surgical implant template, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical implant template, reusable

MOTOBAND Instruments by Crossroads Extremity Systems Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, reusable.

Newclip Instruments — NEWCLIP TECHNICS · Class I
Titan Reverse Shoulder System — Smith & Nephew, Inc. · Class I
Legion — Smith & Nephew, Inc. · Class II
LIGAFIX® — S.B.M. SAS · Class I
EVOS — Smith & Nephew, Inc. · Class I
Tranquil-C™ — NEXUS SPINE, L.L.C. · Class I
VFT — Ldr Spine USA · Class II
Tranquil-C™ — NEXUS SPINE, L.L.C. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Crossroads Extremity Systems Llc

Sources (1)

FDA UDI 264423c4-1d2a-4dda-af27-01b92f51660f 34 fields · synced May 30, 2026